Boston University Alzheimer's Disease Research Center

波士顿大学阿尔茨海默病研究中心

基本信息

  • 批准号:
    10468304
  • 负责人:
  • 金额:
    $ 322.91万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2021
  • 资助国家:
    美国
  • 起止时间:
    2021-08-15 至 2026-06-30
  • 项目状态:
    未结题

项目摘要

The Boston University Alzheimer's Disease Research Center (BU ADRC) is committed to the goals and strategies of NAPA including: to prevent and effectively treat AD and AD related dementias (ADRD) by 2025 by expanding AD/ADRD research; to accelerate efforts to identify early and pre-symptomatic stages of AD/ADRD; and to educate the public about AD/ADRD. BU ADRC research themes are congruent with NIH AD/ADRD Research Summit recommendations including: 1) research on heterogeneity and the multifactorial nature of AD/ADRD; 2) molecular profiling of existing and new cohorts; and 3) developing new public-private partnerships. We operationalize our mission through 7 tightly integrated cores: Administrative, Clinical (CC), Data Management and Statistics (DMS), Biomarker, Neuropathology (NPC), Outreach/Recruitment, Engagement (ORE), Genetics and Molecular Profiling (GMP) and a research education component (REC). The Cores are focused on cutting edge research, proactive community engagement, training the next generation of AD/ADRD clinicians and researchers, and sharing key material, data, and expertise both among key partners and with the community at large. The BU ADRC has made significant contributions to the remarkable growth of AD/ADRD research nationally and has actively contributed participants, biological samples, clinical data, and scientific expertise to all major national AD/ADRD research initiatives. The BU ADRC has been the catalyst for exciting new research on genetic and lifespan environmental risk factors and AD/ADRD, particularly vascular risk and exposure to repetitive head impacts (RHI) from contact sports, military service and other sources. Major BU ADRC research themes include studies on RHI from contact sports and military service and risk for AD/ADRD, including chronic traumatic encephalopathy (CTE) and deep phenotyping AD/ADRD heterogeneity with a range of complementary innovative approaches including digital and EEG phenotyping; neuropathology; genetics; biostatistical modelling; biomarker discovery; and molecular profiling. The BU ADRC will build on this strong record of accomplishment to support new research and educate the next generation of AD/ADRD scientists. The BU ADRC will also support high risk high gain innovative developmental projects focused on NAPA and NIA strategic goals and utilize our collective expertise and experience to facilitate career development of investigators with diverse backgrounds. The BU ADRC will develop new partnerships and enhance current partnerships with other ADRCs and national research programs, foundations, advocacy groups and private organizations in our quest to prevent and treat AD/ADRD. Exposure to RHI is associated with CTE and a wide range of other AD/ADRD pathologies. As recognized leaders in this space, we are uniquely positioned to support research on genetic and other risks factors and study how RHI affects the clinical course, biomarker profile, and clinical-pathological features of AD/ADRD including CTE.
波士顿大学阿尔茨海默病研究中心(BU ADRC)致力于实现这些目标, 国家适应行动方案的战略包括:到2025年预防和有效治疗AD和AD相关痴呆, 扩大AD/ADRD研究;加快努力,以确定AD/ADRD的早期和症状前阶段; 并教育公众有关AD/ADRD的知识。BU ADRC研究主题与NIH AD/ADRD一致 研究峰会的建议包括:1)研究异质性和多因素的性质, AD/ADRD; 2)现有和新队列的分子特征分析;以及3)开发新的公私合作伙伴关系 伙伴关系。我们通过7个紧密集成的核心来实现我们的使命:行政,临床(CC), 数据管理和统计(DMS)、生物标志物、神经病理学(NPC)、外展/招募, 参与(ORE),遗传学和分子分析(GMP)和研究教育部分(REC)。 核心专注于前沿研究,积极主动的社区参与,培训下一个 AD/ADRD临床医生和研究人员的一代,并分享关键材料,数据和专业知识, 主要合作伙伴和整个社区。BU ADRC为以下方面做出了重大贡献: AD/ADRD研究在全国范围内显着增长,并积极贡献参与者,生物 为所有主要的国家AD/ADRD研究计划提供样本、临床数据和科学专业知识。的BU ADRC一直是令人兴奋的遗传和寿命环境风险因素新研究的催化剂, AD/ADRD,特别是血管风险和接触接触性运动、军事的重复性头部撞击(RHI) 服务和其他来源。BU ADRC的主要研究主题包括接触性运动中的RHI研究, 军事服务和AD/ADRD的风险,包括慢性创伤性脑病(CTE)和深 表型AD/ADRD异质性与一系列互补的创新方法,包括数字 和EEG表型;神经病理学;遗传学;生物统计建模;生物标志物发现;和分子生物学 侧写BU ADRC将在这一良好的成就记录基础上,支持新的研究, 培养下一代AD/ADRD科学家。BU ADRC还将支持高风险高收益 创新的发展项目侧重于国家适应行动方案和国家影响评估战略目标,并利用我们的集体专长 和经验,以促进不同背景的调查人员的职业发展。BU ADRC将 发展新的伙伴关系,加强与其他发展成果中心和国家研究机构的现有伙伴关系 项目、基金会、倡导团体和私人组织,以寻求预防和治疗AD/ADRD。 暴露于RHI与CTE和广泛的其他AD/ADRD病理相关。承认的 作为这一领域的领导者,我们在支持遗传和其他风险因素的研究方面具有独特的地位, 研究RHI如何影响AD/ADRD的临床病程、生物标志物特征和临床病理特征 包括CTE。

项目成果

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Ann C. McKee其他文献

In vivo neurotoxicity of beta-amyloid [β(1–40)] and the β(25–35) fragment
β-淀粉样蛋白 [β(1–40)] 和 β(25–35) 片段的体内神经毒性
  • DOI:
  • 发表时间:
    1992
  • 期刊:
  • 影响因子:
    4.2
  • 作者:
    N. Kowall;Ann C. McKee;B. Yankner;M. Beal
  • 通讯作者:
    M. Beal
VA’s National PTSD Brain Bank: a National Resource for Research
  • DOI:
    10.1007/s11920-017-0822-6
  • 发表时间:
    2017-08-25
  • 期刊:
  • 影响因子:
    6.700
  • 作者:
    Matthew J. Friedman;Bertrand R. Huber;Christopher B. Brady;Robert J. Ursano;David M. Benedek;Neil W. Kowall;Ann C. McKee
  • 通讯作者:
    Ann C. McKee
3.39 Identification of Neuropathological Substrates of Neuropsychiatric Symptoms in Adolescent and Young Adult Athletes Using Deep Learning
  • DOI:
    10.1016/j.jaac.2024.08.206
  • 发表时间:
    2024-10-01
  • 期刊:
  • 影响因子:
  • 作者:
    Daniel G. Koenigsberg;Justin Kauffman;Gabriel A. Marx;Andrew T. McKenzie;Timothy E. Richardson;Robina Afzal;Jon Cherry;Jesse Mez;Kurt Farrell;Ann C. McKee;John F. Crary
  • 通讯作者:
    John F. Crary
18F-MK-6240 tau PET in patients at-risk for chronic traumatic encephalopathy
  • DOI:
    10.1186/s13024-025-00808-1
  • 发表时间:
    2025-02-25
  • 期刊:
  • 影响因子:
    17.500
  • 作者:
    Michael L. Alosco;Jhony Mejía Pérez;Julia E. Culhane;Ranjani Shankar;Christopher J. Nowinski;Samantha Bureau;Nidhi Mundada;Karen Smith;Alinda Amuiri;Breton Asken;Jenna R. Groh;Annalise Miner;Erika Pettway;Sydney Mosaheb;Yorghos Tripodis;Charles Windon;Gustavo Mercier;Robert A. Stern;Lea T. Grinberg;David N. Soleimani-Meigooni;Bradley T. Christian;Tobey J. Betthauser;Thor D. Stein;Ann C. McKee;Chester A. Mathis;Eric E. Abrahamson;Milos D. Ikonomovic;Sterling C. Johnson;Jesse Mez;Renaud La Joie;Daniel Schonhaut;Gil D. Rabinovici
  • 通讯作者:
    Gil D. Rabinovici
Chronic Traumatic Encephalopathy: Where Are We and Where Are We Going?

Ann C. McKee的其他文献

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{{ truncateString('Ann C. McKee', 18)}}的其他基金

Boston University Alzheimer's Disease Research Center
波士顿大学阿尔茨海默病研究中心
  • 批准号:
    10652548
  • 财政年份:
    2021
  • 资助金额:
    $ 322.91万
  • 项目类别:
Core D: Neuropathology Core
核心 D:神经病理学核心
  • 批准号:
    10652567
  • 财政年份:
    2021
  • 资助金额:
    $ 322.91万
  • 项目类别:
Core D: Neuropathology Core
核心 D:神经病理学核心
  • 批准号:
    10264291
  • 财政年份:
    2021
  • 资助金额:
    $ 322.91万
  • 项目类别:
Core D: Neuropathology Core
核心 D:神经病理学核心
  • 批准号:
    10468309
  • 财政年份:
    2021
  • 资助金额:
    $ 322.91万
  • 项目类别:
Neuropath Core
神经病核心
  • 批准号:
    10468283
  • 财政年份:
    2020
  • 资助金额:
    $ 322.91万
  • 项目类别:
CTBI:CBI Tauopathy in Mice and Human: Neurodegeneration after Repetitive Neurotrauma: Mechanisms and Biomarker Discovery
CTBI:小鼠和人类的 CBI Tau 蛋白病:重复性神经创伤后的神经变性:机制和生物标志物发现
  • 批准号:
    10436771
  • 财政年份:
    2020
  • 资助金额:
    $ 322.91万
  • 项目类别:
CTBI:CBI Tauopathy in Mice and Human: Neurodegeneration after Repetitive Neurotrauma: Mechanisms and Biomarker Discovery
CTBI:小鼠和人类的 CBI Tau 蛋白病:重复性神经创伤后的神经变性:机制和生物标志物发现
  • 批准号:
    10553627
  • 财政年份:
    2020
  • 资助金额:
    $ 322.91万
  • 项目类别:
Neuropath Core
神经病核心
  • 批准号:
    10047357
  • 财政年份:
    2020
  • 资助金额:
    $ 322.91万
  • 项目类别:
Neuropath Core
神经病核心
  • 批准号:
    10670334
  • 财政年份:
    2020
  • 资助金额:
    $ 322.91万
  • 项目类别:
Neuropath Core
神经病核心
  • 批准号:
    10256772
  • 财政年份:
    2020
  • 资助金额:
    $ 322.91万
  • 项目类别:

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